A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7668n54



Internal ID22775563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63540916..63594155hg38UCSC Ensembl
chr20:62172269..62225508hg19UCSC Ensembl
chr20:61642713..61695952hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3853240
hg1953240
hg1853240
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv586577, nsv586575, nsv586576
SamplesHGDP00899
Known GenesC20orf195, GMEB2, HELZ2, SRMS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7668n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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